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Neolens, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K882814
NEOLENS PRESCRIPTION SPECTACLE LENS
July 29, 1988
K882813
NEOLENS SUNGLASSES
July 29, 1988